Chen Xian-Ming, O'Hara Steven P, Huang Bing Q, Nelson Jeremy B, Lin Jim Jung-Ching, Zhu Guan, Ward Honorine D, LaRusso Nicholas F
Center for Basic Research in Digestive Diseases, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Infect Immun. 2004 Dec;72(12):6806-16. doi: 10.1128/IAI.72.12.6806-6816.2004.
The apical organelles in apicomplexan parasites are characteristic secretory vesicles containing complex mixtures of molecules. While apical organelle discharge has been demonstrated to be involved in the cellular invasion of some apicomplexan parasites, including Toxoplasma gondii and Plasmodium spp., the mechanisms of apical organelle discharge by Cryptosporidium parvum sporozoites and its role in host cell invasion are unclear. Here we show that the discharge of C. parvum apical organelles occurs in a temperature-dependent fashion. The inhibition of parasite actin and tubulin polymerization by cytochalasin D and colchicines, respectively, inhibited parasite apical organelle discharge. Chelation of the parasite's intracellular calcium also inhibited apical organelle discharge, and this process was partially reversed by raising the intracellular calcium concentration by use of the ionophore A23187. The inhibition of parasite cytoskeleton polymerization by cytochalasin D and colchicine and the depletion of intracellular calcium also decreased the gliding motility of C. parvum sporozoites. Importantly, the inhibition of apical organelle discharge by C. parvum sporozoites blocked parasite invasion of, but not attachment to, host cells (i.e., cultured human cholangiocytes). Moreover, the translocation of a parasite protein, CP2, to the host cell membrane at the region of the host cell-parasite interface was detected; an antibody to CP2 decreased the C. parvum invasion of cholangiocytes. These data demonstrate that the discharge of C. parvum sporozoite apical organelle contents occurs and that it is temperature, intracellular calcium, and cytoskeleton dependent and required for host cell invasion, confirming that apical organelles play a central role in C. parvum entry into host cells.
顶复门寄生虫中的顶端细胞器是含有复杂分子混合物的特征性分泌囊泡。虽然已证明顶端细胞器的释放参与了一些顶复门寄生虫的细胞入侵,包括刚地弓形虫和疟原虫属,但微小隐孢子虫子孢子顶端细胞器释放的机制及其在宿主细胞入侵中的作用尚不清楚。在此,我们表明微小隐孢子虫顶端细胞器的释放以温度依赖的方式发生。细胞松弛素D和秋水仙碱分别抑制寄生虫肌动蛋白和微管蛋白聚合,从而抑制寄生虫顶端细胞器的释放。螯合寄生虫细胞内的钙也抑制顶端细胞器的释放,并且通过使用离子载体A23187提高细胞内钙浓度可部分逆转这一过程。细胞松弛素D和秋水仙碱对寄生虫细胞骨架聚合的抑制以及细胞内钙的耗竭也降低了微小隐孢子虫子孢子的滑行运动能力。重要的是,微小隐孢子虫子孢子对顶端细胞器释放的抑制阻止了寄生虫对宿主细胞(即培养的人胆管细胞)的入侵,但不影响其对宿主细胞的附着。此外,在宿主细胞 - 寄生虫界面区域检测到一种寄生虫蛋白CP2向宿主细胞膜的转运;抗CP2抗体减少了微小隐孢子虫对胆管细胞的入侵。这些数据表明微小隐孢子虫子孢子顶端细胞器内容物的释放是存在的,并且它是温度、细胞内钙和细胞骨架依赖性的,是宿主细胞入侵所必需的,证实了顶端细胞器在微小隐孢子虫进入宿主细胞过程中起核心作用。